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Substrate specificity of NO synthases: Detailed comparison of L-arginine, homo-L-arginine, their N-omega-hydroxy derivatives, and N-omega-hydroxynor-L-arginine

机译:NO合酶的底物特异性:L-精氨酸,同型L-精氨酸,它们的N-ω-羟基衍生物和N-ω-羟基nor-L-精氨酸的详细比较

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A detailed comparison of the oxidation of five compounds closely related to L-arginine (Arg) by purified recombinant neuronal and macrophage NO synthases (NOS I and NOS II) was performed. Homo-L-arginine (homo-Arg) is oxidized by both NOSs in the presence of NADPH with major formation of NO and homo-L-citrulline, with a molar ratio of close to 1, and minor formation of N-omega-hydroxyhomo-L-arginine (homo-NOHA). Oxidation of homo-NOHA by the two NOSs also leads to NO and homocitrulline in a 1:1 molar ratio. On the contrary, N-omega-hydroxynor-L-arginine (nor-NOHA) is a very poor substrate of NOS I and II, which fails to produce significant amounts of nitrite. The catalytic efficiency of both NOSs markedly decreases in the order Arg > NOHA > homo-Arg > homo-NOHA, as shown by the 20- and 10-fold decrease of k(cat)/K-m observed for NOS I and NOS II, respectively, when comparing Arg to homo-NOHA. The greater loss of catalytic efficiency for homo-Arg, when compared to that for Arg, appears to occur at the first step (N-hydroxylation) of the reaction. In that regard, it is noteworthy that the V-m values for NOHA and homo-NOHA oxidation are very similar (about 1 and 2 mu mol of NO min(-1) mg of protein(-1) for NOS I and II, respectively). In fact, lengthening of the Arg chain by one CH2 leads not only to markedly decreased k(cat)/K-m but also to clear disturbances in NOS functioning. This is shown by a greater accumulation of the N-omega-hydroxyguanidine intermediate (homo-NOHA:homocitrulline ratio between 0.2 and 0.4) and an increased consumption of NADPH for NO formation (between 2.0 and 2.6 mol of NADPH consumed for the formation of 1 mol of NO in the case of homo-Arg, instead of 1.5 mol in the case of Arg). Most of the above results could be interpreted by comparing the possible positionings of the various substrates relative to the two NOS active oxygen species which are believed to be responsible for the two steps of the reaction. [References: 57]
机译:对纯化的重组神经元和巨噬细胞NO合酶(NOS I和NOS II)对与L-精氨酸(Arg)密切相关的五种化合物的氧化进行了详细比较。在NADPH的存在下,NOS均将同型L-精氨酸(homo-Arg)氧化,主要形成NO和高L-瓜氨酸,摩尔比接近1,而次要形成N-Omega-hydroxyhomo -L-精氨酸(纯合NOHA)。两种NOS对homo-NOHA的氧化也导致NO和高瓜氨酸的摩尔比为1:1。相反,N-ω-羟基去甲精氨酸(nor-NOHA)是NOS I和II的非常差的底物,无法产生大量的亚硝酸盐。两种NOS的催化效率均按Arg> NOHA> homo-Arg> homo-NOHA的顺序显着降低,这分别由NOS I和NOS II观察到的k(cat)/ Km降低20倍和10倍来表明,将Arg与homo-NOHA进行比较时。与对Arg相比,均Arg的催化效率的更大损失似乎发生在反应的第一步(N-羟基化)。在这方面,值得注意的是,NOHA和均一NOHA氧化的Vm值非常相似(对于NOS I和II,分别约为1和2 mol mol NOmin(-1)mg蛋白质(-1)) 。实际上,一个CH2延长Arg链不仅导致k(cat)/ K-m显着降低,而且还消除了NOS功能的干扰。 N-ω-羟基胍中间体的积累量更大(同型NOHA:高同苯胺比在0.2和0.4之间),而用于形成NO的NADPH消耗量增加(用于形成1的NADPH消耗量在2.0和2.6 mol之间)表明了这一点。在均一Arg的情况下为1mol的NO,而不是在Arg的情况下为1.5mol的NO。可以通过比较各种底物相对于两种NOS活性氧的可能位置来解释上述大多数结果,据信这是反应的两个步骤。 [参考:57]

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